Percutaneous Stabilization of thoracolumbal spine fractures

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00005052

Enrollment

125

Registered

2013-09-23

Start date

2012-05-15

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

spine fracture S32

Interventions

Group 1: Minimal-invasive stabilized patients are followed up 9-12 months postoperatively. Clinical evaluation was performed by subjective evaluation of the final results by patients themselves Group

Eligibility

Sex/Gender

All

Age

16 Years to No maximum

Inclusion criteria

Inclusion criteria: a. Acute (< 3 weeks) traumatic injuries from T1 to L5 with percutaneous internal fixation b.written consent

Exclusion criteria

Exclusion criteria: a. concomitant injuries, which influence spine function b. pediatric fractures c. kyphoplasty d.no written consent

Design outcomes

Primary

Measure	Time frame
Spine function (VAS Spine Score) after implant removal (9-12 months postoperative)	—

Secondary

Measure	Time frame
radiographic evaluation of the segmental kyphosis and the wedging deformity of the involved vertebral body performed during clinical follow up	—

Countries

Germany

Contacts

Public ContactTobias Gensior

Universitätsklinikum Düsseldorf, Klinik für Unfall- und Handchirurgie

tobias.gensior@med.uni-duesseldorf.de0049 211 8104400

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026